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1. Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons

2. Mining impactful discoveries from the biomedical literature

3. A randomized double-blind clinical trial on safety and efficacy of tauroursodeoxycholic acid (TUDCA) as add-on treatment in patients affected by amyotrophic lateral sclerosis (ALS): the statistical analysis plan of TUDCA-ALS trial

4. Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

5. Clinical, Cortical, Subcortical, and White Matter Features of Right Temporal Variant FTD

6. Limbic Network and Papez Circuit Involvement in ALS: Imaging and Clinical Profiles in GGGGCC Hexanucleotide Carriers in C9orf72 and C9orf72-Negative Patients

7. The involvement of language‐associated networks, tracts, and cortical regions in frontotemporal dementia and amyotrophic lateral sclerosis: Structural and functional alterations

8. Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial

9. The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

10. Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival

11. Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

12. Care, burden and self-described positive aspects of caring in amyotrophic lateral sclerosis: an exploratory, longitudinal, mixed-methods study

13. Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data

14. Tauroursodeoxycholic acid in patients with amyotrophic lateral sclerosis: The TUDCA-ALS trial protocol

15. Prediction of caregiver quality of life in amyotrophic lateral sclerosis using explainable machine learning

16. Discrete choice experiment for eliciting preference for health services for patients with ALS and their informal caregivers

17. Toward a Digital Health Intervention for Vestibular Rehabilitation: Usability and Subjective Outcomes of a Novel Platform

18. White matter microstructure alterations in frontotemporal dementia: Phenotype‐associated signatures and single‐subject interpretation

19. Imaging data reveal divergent longitudinal trajectories in PLS, ALS and poliomyelitis survivors: Group-level and single-subject traits

20. Imaging data indicate cerebral reorganisation in poliomyelitis survivors: Possible compensation for longstanding lower motor neuron pathology

21. A Road Map for Remote Digital Health Technology for Motor Neuron Disease

22. Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene

23. Alterations in somatosensory, visual and auditory pathways in amyotrophic lateral sclerosis: an under-recognised facet of ALS

24. Cerebellar remodelling decades after spinal cord insult: neuroplasticity in poliomyelitis survivors

25. MRI data confirm the selective involvement of thalamic and amygdalar nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis

26. Imaging and clinical data indicate considerable disease burden in ‘probable’ PLS: Patients with UMN symptoms for 2–4 years

27. Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland

28. Generation of twelve induced pluripotent stem cell lines from two healthy controls and two patients with sporadic amyotrophic lateral sclerosis

29. Progressive brainstem pathology in motor neuron diseases: Imaging data from amyotrophic lateral sclerosis and primary lateral sclerosis

30. Thalamic, hippocampal and basal ganglia pathology in primary lateral sclerosis and amyotrophic lateral sclerosis: Evidence from quantitative imaging data

31. 'Switchboard' malfunction in motor neuron diseases: Selective pathology of thalamic nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis

32. Informal Caregivers in Amyotrophic Lateral Sclerosis: A Multi-Centre, Exploratory Study of Burden and Difficulties

33. Amyotrophic lateral sclerosis patient iPSC-derived astrocytes impair autophagy via non-cell autonomous mechanisms

34. Survival prediction in Amyotrophic lateral sclerosis based on MRI measures and clinical characteristics

35. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

36. Virtual brain biopsies in amyotrophic lateral sclerosis: Diagnostic classification based on in vivo pathological patterns

37. Generation of six induced pluripotent stem cell (iPSC) lines from two patients with amyotrophic lateral sclerosis (NUIGi043-A, NUIGi043-B, NUIGi043-C, NUIGi044-A, NUIGi044-B, NUIGi044-C)

38. The C9orf72 expansion is associated with accelerated respiratory function decline in a large Amyotrophic Lateral Sclerosis cohort [version 1; peer review: 2 approved]

39. Post-polio Syndrome: More Than Just a Lower Motor Neuron Disease

40. Pathological Crying and Laughing in Motor Neuron Disease: Pathobiology, Screening, Intervention

41. Tracking a Fast-Moving Disease: Longitudinal Markers, Monitoring, and Clinical Trial Endpoints in ALS

42. Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profiling

43. Neurophysiological markers of network dysfunction in neurodegenerative diseases

44. Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging study

45. Dysfunction of attention switching networks in amyotrophic lateral sclerosis

46. CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

47. Genomic signals of migration and continuity in Britain before the Anglo-Saxons

48. Insular Celtic population structure and genomic footprints of migration.

49. Referral bias in ALS epidemiological studies.

50. Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype

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